US4844711A - Hair colorants and methods of coloring hair - Google Patents

Hair colorants and methods of coloring hair Download PDF

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Publication number
US4844711A
US4844711A US07/142,973 US14297388A US4844711A US 4844711 A US4844711 A US 4844711A US 14297388 A US14297388 A US 14297388A US 4844711 A US4844711 A US 4844711A
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Prior art keywords
weight
hair
basic composition
parts
urease
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US07/142,973
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Udo Hoppe
Klaus Korbacher
Karl-Heinz Schrader
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Hans Schwarzkopf and Henkel GmbH
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Beiersdorf AG
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Assigned to HANS SCHWARZKOPF GMBH reassignment HANS SCHWARZKOPF GMBH ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: SCHRADER, KARLHEINZ
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/10Preparations for permanently dyeing the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/11Encapsulated compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42Amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/66Enzymes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/41Particular ingredients further characterized by their size
    • A61K2800/412Microsized, i.e. having sizes between 0.1 and 100 microns
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/52Stabilizers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/88Two- or multipart kits

Definitions

  • the invention therefore relates to a hair colorant based on oxidative dyes, characterized by
  • Reducing agents for example sodium sulphite
  • Solvents for example water or lower alcohols.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)
  • Cleaning And Drying Hair (AREA)

Abstract

A hair colorant based oxidative dyes, in which colorant the alkaline pH necessary for coloring is not produced until during application by enzymatic methods, and a method of coloring hair.

Description

The invention relates to a hair colorant based on oxidative dyes in which the alkaline pH necessary for colouring is first produced during use by enzymatic methods through the action of urease on urea, and a method of colouring hair using such a hair colorant.
To a large extent, colouring of hair is carried out using so-called oxidative dyes since the latter provide a colouring result having intensive colours of high colour fastness. In this method, the oxidative dyes are produced during the colouring process through oxidative coupling of a developer component and a coupler component. Such coupler and developer components for achieving a very wide variety of colour shades, collectively called hair dye intermediates below, are described in large number in the literature.
Although oxidative coupling, i.e. development of the colouring, can in principle also take place by means of atmospheric oxygen, chemical oxidants are employed in most cases. In particular, oxidants based on hydrogen peroxide have proven successful here, preferably addition compounds of hydrogen peroxide with urea, melamine or sodium borate in addition to hydrogen peroxide itself.
For practical application as hair colorants, the dye intermediates are incorporated into a suitable cosmetic base, which can be a solution, a cream or a gel depending on the type of the final product desired. The oxidant is then added to this preparation immediately before application to the hair.
Such hair colorants from the prior art are normally adjusted to an alkaline pH, preferably through addition of ammonia or organic amines, such as, for example, monoethanolamine.
Although this alkaline pH of conventional hair-care agents leads to a smooth course of the colour-forming oxidation reaction and also to good take-up of the hair dye as a consequence of swelling of the hair in the alkaline medium, it also has not inconsiderable disadvantages: due to the considerable deviation from the skin-physiological, slightly acidic pH, the head skin and the hair are subjected to very hostile conditions. For the same reason, application of such a hair colorant using unprotected hands is not possible without further measures, which makes self-application to the hair and application other than in a hairdressing salon more difficult.
The present invention therefore had the object of providing a hair colorant based on oxidative dyes which, compared with the prior art, causes lower alkali exposure of the hair and is thus also milder and is better tolerated by the skin, and at the same time the colouring result is of at least equal or better quality.
Surprisingly, it has now been found that such a hair colorant can be provided by selecting a composition in which, starting from a basic composition buffered in the acidic region, the alkaline pH is first produced during the colouring process by enzymatic methods through the action of urease on urea.
The invention therefore relates to a hair colorant based on oxidative dyes, characterized by
(a) a basic composition which is buffered in the acidic region by means of a suitable buffer mixture and which, in addition, contains the hair dye intermediates and urea,
(b) urease, and
(c) an oxidant which releases hydrogen peroxide and which is microencapsulated in an acid-stable material which is soluble in alkaline media,
the three components (a), (b) and (c) first being mixed immediately prior to the colouring process.
The basic composition of the hair colorant according to the invention is a gel, a cream or a surfactant-containing, foaming solution, such as, for example, a shampoo, depending on the type of the final product desired. This basic material contains, in amounts which are conventional for this purpose, the components which are known from the prior art and which are suitable for application to hair. Components of such basic compositions are, for example:
wetting agents and emulsifiers, such as ionic and nonionic surfactants, for example alkylsulphonates, fatty alcohol sulphates, fatty alcohol polyglycol ether sulphates, ethoxylation products of fatty alcohols, fatty acids
or alkylphenols, sorbitan fatty acid esters, fatty acid partial glycerides and fatty acid alkanolamides.
Thickeners, for example cellulose derivatives, starch, fatty alcohols, paraffin oils and fatty acids.
Reducing agents, for example sodium sulphite
Perfume oils
Hair-care additives, for example water-soluble cationic polymers, protein derivatives, lecithin, cholesterol and pantothenic acid
Solvents, for example water or lower alcohols.
According to the invention, the basic composition is adjusted to an acidic pH, preferably in the pH range 4.9-6.9, in particular in the pH range 6.0-6.8, by means of a buffer mixture. The proportion of buffer mixture in the basic composition is preferably 2-25% by weight. Preferably suitable buffer mixtures are citrate or phosphate buffers, it being possible for the components of the buffer mixture either to be admixed as pure substances with the remaining components of the basic composition or to be added as an aqueous solution.
In particular, the buffer mixture employed is an aqueous solution which contains 0.7-1.0% by weight of citric acid and 3.4-4.3% by weight of diammonium hydrogen phosphate, in a particularly preferred embodiment having a citric acid:diammonium hydrogen phosphate ratio of 1:4.4-1:4.9.
In addition, the basic composition of the hair colorant according to the invention contains urea in an amount of preferably 2-20% by weight, in particular 2 to 6% by weight.
Furthermore, the basic composition contains the hair dye intermediates, more specifically, according to the invention, preferably containing 0.01 to 5.0% by weight, in particular 0.05 to 3.0% by weight, of one or more conventional developer components and preferably 0.01 to 3.0% by weight, in particular 0.05 to 2.0% by weight, of one or more conventional coupler components. The developer component(s) : coupler component(s) molar ratio in the hair colorant according to the invention is generally about 1:1, but an excess of one or other hair dye intermediates is not disadvantageous.
In the context of the invention, all conventional developer and coupler components which are known to those skilled in the art can in principle be employed, but, depending on the colour desired to be conferred, the developer component(s) are selected from the group comprising the p-toluylenediamines, the p-phenylenediamines, the 2,5-diaminopyridines or the p-aminophenols as the free base or in the form of a cosmetically acceptable salt, and the coupler component(s) are selected from the group comprising the resorcinols, the m-aminophenols, the m-phenylenediamines, the 2,3-diamino-6-methoxypyridines or alpha-naphthol.
In order to produce specific colour shades, it may in addition be expedient to add to the basic composition according to the invention small amounts of one or more direct-action hair dyes in addition to the hair dye intermediates mentioned above.
The second component of the hair colorant according to the invention is the enzyme urease, in an amount of preferably 0.01 to 0.20 parts by weight, in particular 0.05 to 0.15 parts by weight, per 100 parts by weight of the basic composition. In a specific embodiment of the invention, which is particularly suitable for colouring when "greasy" hair shafts are present, component (b) is the enzyme urease, preferably in the abovementioned amounts, mixed with the enzyme lipase, the lipase being employed in an amount from preferably 0.01 to 0.1 part by weight, in particular 0.03 to 0.08 part by weight, per 100 parts by weight of the basic composition, and the two enzymes preferably being mixed in the dry form. In a further specific embodiment of the invention, the enzyme or the enzyme mixture can be employed diluted with an inert solid, for example finely divided silicon dioxide.
The third component of the hair colorant according to the invention comprises a microencapsulated oxidant which releases hydrogen peroxide, preferably an addition product of hydrogen peroxide on urea, melamine or sodium borate, in particular sodium percarbonate or carbamide peroxide. It is essential for the present invention that a material is used for the microencapsulation which is stable in an acidic environment and that the encapsulated oxidant is only liberated at an alkaline pH, since the urease would otherwise be prematurely deactivated. In a preferred fashion according to the invention, alkali-soluble acrylic resins are therefore employed for the microencapsulation of the oxidant. Such materials are commercially available, for example, under the name EudragitR S (Messrs. Rohm, Darmstadt). The hair colorant according to the invention preferably contains 5-15 parts by weight, in particular 8-11 parts by weight, of the microencapsulated, hydrogen peroxide-releasing oxidant per 100 parts by weight of the basic composition.
The three components are prepared separately and until use stored in separate packages, or preferably in a suitable 3-component pack, so that they cannot come into direct contact with one another.
The basic composition is prepared by initially mixing all components with the exception of the hair dye intermediates, to give a homogeneous mixture, preferably with gentle warming, in particular at temperatures from 30°-50° C. In specific cases, it may be expedient to first prepare a mixture of urea and buffer mixture, which is then combined with the remaining components. The hair dye intermediates are preferably then incorporated into the mixture thus obtained.
The urease or the urease/lipase mixture prepared by dry mixing is present in the form of a finely divided powder, which is mixed, if appropriate, with the solid used as diluent.
The hydrogen peroxide-releasing oxidant is microencapsulated by a conventional process, preferably using the fluidized bed process.
Hair-colouring using the hair colorant according to the invention is carried out by mixing the 3 components immediately before use and subsequently applying and distributing the mixture on the hair. As is known to those skilled in the art, the necessary amount of hair colorant depends on the length of hair to be coloured. The application temperatures are preferably in a range from 15°-40° C. After allowing a time of preferably 15-45 minutes, in particular 20-35 minutes, for the hair colorant to act, it is removed by rinsing, and the hair is then washed, if appropriate, using a mild shampoo, rinsed again, and dried.
The hair colorant according to the invention is milder and better tolerated compared to hair colorants known hitherto, without the colouring result having to suffer. On the contrary, improved colouring is apparent in the region of the growing hair roots when the colorant according to the invention is used. A further advantage is the reduced problem of odours caused by the ammonia odour occurring during application.
The following examples are intended to illustrate the invention without representing a limitation (PW denotes parts by weight).
EXAMPLE 1 Colouring gel:
The basic composition is prepared by mixing the belowmentioned components while warming gently (40°):
______________________________________                                    
Raw material             % by weight                                      
______________________________________                                    
Sodium sulphite              0.60                                         
Isopropyl alcohol            10.00                                        
Coconut fatty acid polydiethanolamide                                     
                             35.00                                        
Perfume oil composition      1.30                                         
Buffer solution              20.00                                        
Urea                         5.00                                         
Cetyltrimethylammonium chloride                                           
                             10.00                                        
(30% strength)                                                            
p-Phenylenediamine dihydrochloride                                        
                             0.07                                         
alpha-Naphthol               0.04                                         
Chlororesorcinol             0.04                                         
Water                  to    100.00                                       
______________________________________                                    
During this preparation, the hair dye intermediates p-phenylenediamine dihydrochloride, alpha-naphthol and chlororesorcinol are the last to be incorporated into the solution of the remaining components.
The buffer solution used is an aqueous solution containing 0.95% by weight of citric acid and 4.30% by weight of diammonium hydrogen phosphate.
The basic composition has a pH of 6.5.
Immediately before use, 0.07 PW of urease and 8.6 PW of microencapsulated carbamide peroxide are added per 100 PW of the basic composition, and the components are mixed and applied to the hair. For one hair colouring operation, about 50 g of basic composition and the corresponding amounts of urease and carbamide peroxide are required. The result is a light-blond colour on white hair.
Due to the reaction of urease and urea, the pH increases from 6.5 initially (basic composition) to 8.9 to 9.1.
EXAMPLE 2 Colouring shampoo, light blond:
The basic composition has the following composition:
______________________________________                                    
Raw material             % by weight                                      
______________________________________                                    
Sodium sulphite              0.44                                         
Isopropyl alcohol            7.34                                         
Perfume oil composition      0.73                                         
EDTA                         0.15                                         
Condensation product of C12-C18-fatty                                     
                             55.04                                        
alcohol with 3 moles of ethylene oxide                                    
Urea                         5.62                                         
Buffer solution (analogous to Example 1)                                  
                             22.48                                        
p-Phenylenediamine dihydrochloride                                        
                             0.22                                         
Resorcinol                   0.009                                        
p-Nitro-o-aminophenol        0.11                                         
o-Nitro-p-phenylenediamine   0.01                                         
Water                  to    100.00                                       
______________________________________                                    
The composition is prepared by initially mixing the 5 first-mentioned components. The buffer solution, mixed with the urea, and then the hair dye intermediates are subsequently added, and all components are mixed homogeneously.
Immediately before use, 0.1 PW of urease, 0.05 PW of lipase and 9.0 PW of microencapsulated carbamide peroxide are added per 100 PW of basic composition, and the components are mixed and applied to the hair.
EXAMPLE 3 Hair dye:
The basic composition has the following composition:
______________________________________                                    
Raw material             % by weight                                      
______________________________________                                    
Sodium sulphite              0.50                                         
Cetyl/stearyl alcohol        10.50                                        
Sodium cetylstearylsulphate  1.50                                         
Paraffin oil perliquidum     7.50                                         
Wool wax alcohol             3.75                                         
EDTA                         0.22                                         
Perfume oil composition      0.45                                         
Urea                         5.00                                         
Buffer solution (analogous to Example 1)                                  
                             20.00                                        
p-Toluylenediamine sulphate  1.00                                         
m-Phenylenediamine           0.50                                         
Water                  to    100.00                                       
______________________________________                                    
The composition is prepared by initially mixing the 7 first-mentioned components with the water. The buffer solution, mixed with the urea, and then the hair dye intermediates are subsequently added, and all components are mixed homogeneously. The basic composition has a pH of 6.3.
Application takes place as described in Example 1, 0.1 PW of urease, 0.05 PW of lipase and 9.0 PW of carbamide peroxide being added per 100 PW of the basic composition. The result is a blue colouring on white human hair.
EXAMPLE 4 Colouring shampoo gel:
The basic composition has the following composition:
______________________________________                                    
Raw material             % by weight                                      
______________________________________                                    
Condensation product of nonylphenol with                                  
                         27.00                                            
4 moles of ethylene oxide                                                 
Condensation product of nonylphenol with                                  
                         23.00                                            
9 moles of ethylene oxide                                                 
Isopropyl alcohol        16.44                                            
Ammonium hydroxide, 25% strength                                          
                         11.00                                            
p-Toluylenediamine       1.40                                             
m-Phenylenediamine       0.05                                             
Resorcinol               0.06                                             
m-Aminophenol            0.22                                             
p-Aminophenol            0.23                                             
Ethylenediaminetetraacetic acid                                           
                         0.2                                              
Urea                     2.0                                              
Sodium sulphite          1.0                                              
Water                    15.3                                             
Citric acid              0.38                                             
Diammonium hydrogen phosphate                                             
                         1.72                                             
______________________________________                                    
In order to prepare the basic composition, all raw materials are homogeneously mixed consecutively at about 40° C.
This basic composition is mixed immediately before use with 9 PW of microencapsulated carbamide peroxide, 0.1 PW of urease and 0.05 PW of lipase, and the mixture is applied to the hair. A brown-red gel, which is active for colouring for about 30 minutes, is obtained while the pH increases slowly. 90% white hair is coloured chestnut brown.

Claims (8)

We claim:
1. Hair colorant based on oxidative dyes, characterized by
(a) a basic composition which is buffered in the acidic region by means of a suitable buffer mixture and which, in addition, contains the hair dye intermediates and 2-20% by weight of urea,
(b) 0.01 to 0.20 parts by weight of urease per 100 parts by weight of the basic composition, and
(c) 5 to 15 parts by weight, per 100 parts by weight of the basic composition, of an oxidant which releases hydrogen peroxide and which is microencapsulated in an acid-stable material, the microcapsules being soluble in alkaline media, and releasing hydrogen peroxide subsequent to an increase in pH resulting from the reaction of urea and urease,
the three components (a), (b) and (c) first being mixed immediately prior to the colouring process.
2. Hair colorant according to claim 1, characterized in that the basic composition is buffered at a pH of 4.9-6.9.
3. Hair colorant according to claim 1, characterized in that it contains, as components (b), a mixture of urease and lipase, the lipase being employed in an amount from 0.01 to 0.1 part by weight, relative to 100 parts by weight of the basic composition.
4. Hair colorant according to claim 1, characterized in that the hydrogen peroxide-releasing oxidant is sodium percarbonate or carbamide peroxide.
5. Hair colorant according to claim 1, characterized in that the buffer mixture employed is an aqueous solution of 0.7 to 1.0% by weight of citric acid and 3.4 to 4.3% by weight of diammonium hydrogen phosphate in an amount of 2 to 25% by weight of the basic composition.
6. Process for colouring hair using oxidative dyes, characterized in that a colorant according to claim 1 is applied to the hair and rinsed out after allowing 15-45 minutes for the colorant to act, and the hair is washed, if appropriate, rinsed again and subsequently dried.
7. Hair colorant according to claim 1, characterized in that it contains 0.005 to 0.15 part by weight of urease per 100 parts by weight of the basic composition.
8. Hair colorant according to claim 1, characterized in that it contains 8-11 parts by weight of the microencapsulated, hydrogen peroxide-releasing oxidant per 100 parts by weight of the basic composition.
US07/142,973 1987-01-16 1988-01-12 Hair colorants and methods of coloring hair Expired - Fee Related US4844711A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19873701098 DE3701098A1 (en) 1987-01-16 1987-01-16 HAIR DYE AND METHOD FOR HAIR DYE
DE3701098 1987-01-16

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EP (1) EP0274701B1 (en)
JP (1) JPH0745391B2 (en)
KR (1) KR880008794A (en)
AT (1) ATE69946T1 (en)
DE (2) DE3701098A1 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5053051A (en) * 1988-01-21 1991-10-01 Goldwell Gmbh Means and method for the oxidative dyeing, especially the redyeing, of living hair: micro-encapsulated acid
US5554197A (en) * 1994-07-19 1996-09-10 Anthony Bernard Incorporated Hair dying system and methods for accurately blending and developing hair dye
ES2131462A1 (en) * 1997-04-01 1999-07-16 Alfaro M Dolores Garcia Procedure for reducing the percentages of hydrogen peroxide in dyeing and bleaching operations in hairdressing.
DE19824073A1 (en) * 1998-05-29 1999-12-02 Beiersdorf Ag Enzyme-containing cosmetic or dermatological preparations, used for care of the hair and scalp, especially for preventing greasy hair
US8343238B1 (en) 2011-12-30 2013-01-01 L'oreal Sa. Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases
US8506651B2 (en) 2011-12-30 2013-08-13 L'oreal S.A. Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases
US8556994B2 (en) 2011-12-30 2013-10-15 L'oreal Process for altering the appearance of hair using a composition containing direct dyes and non-hydroxide bases
US8591872B2 (en) 2011-12-30 2013-11-26 L'oreal Composition and process for reducing the curl and frizziness of hair
US10596100B2 (en) 2012-12-19 2020-03-24 L'oreal Cosmetic compositions containing an alkoxysilane and a silsesquioxane resin

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19612866A1 (en) * 1996-03-30 1997-10-30 Henkel Kgaa Process for the automatic displacement of the pH of an aqueous treatment solution and solid detergents suitable therefor
DE102004042097A1 (en) * 2004-08-30 2006-03-09 Henkel Kgaa Agent for dyeing keratinous fibers
KR101005316B1 (en) * 2008-02-05 2011-01-05 주식회사 수안향장 Dyeing Composition for Hair with hardwood charcoal powder
ES2672775T3 (en) * 2008-05-06 2018-06-18 Basf Se Polyurethanes as rheology modifying agents for cosmetic preparations
JP2014189528A (en) * 2013-03-28 2014-10-06 Milbon Co Ltd Hair cosmetic
DE102021202087A1 (en) * 2021-03-04 2022-09-08 Henkel Ag & Co. Kgaa Process for coloring keratinous material, comprising the use of an organosilicon compound, a coloring compound, a sealing agent and an enzyme-containing pretreatment agent

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE124794C (en) * 1900-01-01
US2817342A (en) * 1953-12-17 1957-12-24 Colgate Palmolive Co Method of permanently reshaping a keratin-containing substance
DE1229980B (en) * 1960-08-30 1966-12-08 Schwarzkopf Fa Hans Permanent wave method
GB1295038A (en) * 1969-02-04 1972-11-01
US3839220A (en) * 1968-10-23 1974-10-01 Mennen Co Microcapsules for use in pressurized systems
US3957424A (en) * 1971-10-27 1976-05-18 The Procter & Gamble Company Enzyme-activated oxidative process for coloring hair
US4129415A (en) * 1976-10-15 1978-12-12 American Cyanamid Company Method for removing permanent dyes from hair and other keratinaceous materials
US4331167A (en) * 1979-02-12 1982-05-25 Wella Aktiengesellschaft Compositions and methods for permanent waving of hair
US4466806A (en) * 1980-08-08 1984-08-21 L'oreal Dyeing compositions containing 3-amino-4-nitroanisole derivatives and their use in dyeing keratin fibres as well as certain new said derivatives

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1242794C2 (en) * 1964-03-03 1974-10-24 Johannes Saphir Process for making permanent waves
IT1013014B (en) * 1970-11-09 1977-03-30 Procter & Gamble SOLUTION FOR DYING HAIR AND COMPOSITION USED IN IT
US3898032A (en) * 1971-06-11 1975-08-05 Zotos Int Inc Oxidative hair-coloring mixtures containing a conditioning agent

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE124794C (en) * 1900-01-01
US2817342A (en) * 1953-12-17 1957-12-24 Colgate Palmolive Co Method of permanently reshaping a keratin-containing substance
DE1229980B (en) * 1960-08-30 1966-12-08 Schwarzkopf Fa Hans Permanent wave method
US3839220A (en) * 1968-10-23 1974-10-01 Mennen Co Microcapsules for use in pressurized systems
GB1295038A (en) * 1969-02-04 1972-11-01
US3957424A (en) * 1971-10-27 1976-05-18 The Procter & Gamble Company Enzyme-activated oxidative process for coloring hair
US4129415A (en) * 1976-10-15 1978-12-12 American Cyanamid Company Method for removing permanent dyes from hair and other keratinaceous materials
US4331167A (en) * 1979-02-12 1982-05-25 Wella Aktiengesellschaft Compositions and methods for permanent waving of hair
US4466806A (en) * 1980-08-08 1984-08-21 L'oreal Dyeing compositions containing 3-amino-4-nitroanisole derivatives and their use in dyeing keratin fibres as well as certain new said derivatives

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Hackh s Chemical Dictionary 4th Edition, 1969, Enzyme , p. 242. *
Hackh's Chemical Dictionary 4th Edition, 1969, "Enzyme", p. 242.

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5053051A (en) * 1988-01-21 1991-10-01 Goldwell Gmbh Means and method for the oxidative dyeing, especially the redyeing, of living hair: micro-encapsulated acid
US5554197A (en) * 1994-07-19 1996-09-10 Anthony Bernard Incorporated Hair dying system and methods for accurately blending and developing hair dye
ES2131462A1 (en) * 1997-04-01 1999-07-16 Alfaro M Dolores Garcia Procedure for reducing the percentages of hydrogen peroxide in dyeing and bleaching operations in hairdressing.
DE19824073A1 (en) * 1998-05-29 1999-12-02 Beiersdorf Ag Enzyme-containing cosmetic or dermatological preparations, used for care of the hair and scalp, especially for preventing greasy hair
US8343238B1 (en) 2011-12-30 2013-01-01 L'oreal Sa. Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases
US8506651B2 (en) 2011-12-30 2013-08-13 L'oreal S.A. Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases
US8556994B2 (en) 2011-12-30 2013-10-15 L'oreal Process for altering the appearance of hair using a composition containing direct dyes and non-hydroxide bases
US8591872B2 (en) 2011-12-30 2013-11-26 L'oreal Composition and process for reducing the curl and frizziness of hair
US10596100B2 (en) 2012-12-19 2020-03-24 L'oreal Cosmetic compositions containing an alkoxysilane and a silsesquioxane resin
US11324689B2 (en) 2012-12-19 2022-05-10 L'oreal Cosmetic compositions containing an alkoxysilane and a silsesquioxane resin

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JPS63174918A (en) 1988-07-19
KR880008794A (en) 1988-09-13
EP0274701A2 (en) 1988-07-20
DE3701098A1 (en) 1988-07-28
EP0274701A3 (en) 1988-11-17
JPH0745391B2 (en) 1995-05-17
DE3775024D1 (en) 1992-01-16
ATE69946T1 (en) 1991-12-15
EP0274701B1 (en) 1991-12-04

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